Canonical Allele Identifier: CA351050276

Gene: SAG

Linked Data

• MyVariant Identifiers: chr2:g.234255469T>G (hg19) ; chr2:g.233346823T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346823T>G , CM000664.2:g.233346823T>G	GRCh38
NC_000002.11:g.234255469T>G , CM000664.1:g.234255469T>G	GRCh37
NC_000002.10:g.233920208T>G	NCBI36
NG_009116.1:g.44161T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1129T>G MANE Select	ENSP00000386444.1:p.Leu377Val
ENST00000409110.5:c.1129T>G	ENSP00000386444.1:p.Leu377Val
ENST00000412969.6:n.2349T>G
ENST00000471884.5:n.3160T>G
ENST00000474220.5:n.335T>G
ENST00000476500.5:n.6428T>G
ENST00000492629.1:n.90T>G
NM_000541.4:c.1129T>G	NP_000532.2:p.Leu377Val
XM_011511589.1:c.1129T>G	XP_011509891.1:p.Leu377Val
XM_011511590.1:c.1129T>G	XP_011509892.1:p.Leu377Val
XM_011511591.1:c.1119T>G	XP_011509893.1:p.Ile373Met
XM_011511592.1:c.973T>G	XP_011509894.1:p.Leu325Val
XM_011511593.1:c.829T>G	XP_011509895.1:p.Leu277Val
XM_011511594.1:c.757T>G	XP_011509896.1:p.Leu253Val
XM_011511596.1:c.727T>G	XP_011509898.1:p.Leu243Val
XM_011511597.1:c.727T>G	XP_011509899.1:p.Leu243Val
XR_922978.1:n.1446T>G
XR_922979.1:n.1450T>G
XR_922980.1:n.1545T>G
XM_011511593.3:c.829T>G	XP_011509895.1:p.Leu277Val
XM_017004641.1:c.1119T>G	XP_016860130.1:p.Ile373Met
XM_024453036.1:c.717T>G	XP_024308804.1:p.Ile239Met
XR_001738882.1:n.1327T>G
XR_922980.2:n.1545T>G
NM_000541.5:c.1129T>G MANE Select	NP_000532.2:p.Leu377Val